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Файл:Ординатура / Хирургия / Библиотека им академика М.И. Перельмана / Книга_5882_Библиотеки_им_академика_М_И_Перельмана.pdf
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- •Carbon Based Nanomaterials for Drug Delivery
- •Preface
- •Acknowledgements
- •Contents
- •Editor and Contributors
- •Abbreviations
- •1.2 Market Statistics
- •Carbon-Based Nanomaterials: An Overview
- •1. Introduction
- •1.1 Evolution of Carbon-Based Nanomaterials
- •2. Carbon-Based Nanostructures
- •2.1 Fullerene
- •2.2 Carbon Nanotubes (CNTs)
- •2.4 Graphene
- •2.5 Nanodiamonds (NDs)
- •2.6 Nano-Onions (CNOs)
- •2.7 Nanohorns (CNHs)
- •2.8 Carbon Dots (CDs)
- •2.9 Nanoporous Activated Carbon
- •3. Synthesis Techniques
- •4. Properties of Carbon-Based Nanomaterials
- •4.1 Physicochemical Properties
- •4.2 Thermal Properties
- •4.3 Mechanical Properties
- •4.4 Optoelectronic Properties
- •4.5 Antimicrobial Properties
- •4.6 Biological Properties
- •5. Applications of Carbon-Based Nanomaterials
- •5.1 Environmental Remediation
- •5.2 Agriculture
- •5.3 Biofuel
- •5.4 Energy Storage
- •5.5 Biomedical Applications
- •6. Challenges and Future Perspectives
- •7. Concluding Remarks
- •References
- •Carbon-Based Nanostructured Materials: Designing, Properties and Applications
- •1. Introduction
- •2.1 Zero-Dimensional Carbon-Based Nanostructures (0D)
- •2.2 One-Dimensional Carbon-Based Nanostructures
- •2.3 Two-Dimensional (2D) Carbon-Based Nanostructures
- •2.4 Three-Dimensional (3D) Carbon-Based Nanostructures
- •3.1 Chemical Vapor Deposition
- •3.2 Hydrothermal and Solvothermal Techniques
- •3.3 Microwave-Assisted Technique
- •3.4 Chemical Oxidation Synthesis
- •4. Properties of Carbon-Based Nanostructured Materials
- •4.1 Thermal Properties
- •4.2 Mechanical Properties
- •4.3 Optoelectronic Properties
- •4.4 Antimicrobial Properties
- •4.5 Biological Properties
- •5. Applications of Carbon-Based Nanostructured Materials
- •5.2 Antibacterial and Antiviral Applications
- •5.3 Theragnostic
- •5.4 Wound Healing
- •5.5 Tissue Engineering
- •5.6 Drug Delivery
- •5.7 Biosensing
- •6. Challenges and Future Perspectives
- •7. Concluding Remarks
- •References
- •Drug Delivery System and Technologies
- •1. Introduction
- •2. Drug Delivery System
- •2.1 Conventional Drug Delivery System
- •2.2 Advanced Drug Delivery System
- •2.3 Controlled and Sustainable Drug Delivery System
- •3. Drug Delivery Technologies
- •3.1 Active and Passive Drug Delivery
- •3.2 Smart Drug Delivery
- •3.3 Intravenous and Extravaneous Drug Delivery
- •3.4 Various Types of Delivery Technologies
- •4. Challenges and Future Perspectives
- •5. Conclusion
- •References
- •Carbon-Based Nanomaterials for Drug Delivery: Past, Present, Future Directions
- •1. Introduction
- •3. Current Status in Drug Delivery by CNMs
- •3.1 Graphene-Based Nanomaterials in Drug Delivery
- •3.4 Nanodiamond Based Drug Delivery Systems
- •3.5 Nano-Onions in Drug Delivery
- •3.6 Nanohorns in Drug Delivery
- •3.7 Fullerene in Drug Delivery
- •4. Challenges and Future Perspective
- •5. Conclusions
- •References
- •Carbon Nanomaterial-Incorporated Supramolecular Drug Delivery
- •1. Introduction
- •2. Different Carbon Nanomaterials in Drug Delivery
- •2.1 Carbon Nanotubes (CNTs)
- •2.3 Graphene
- •2.4 Carbon Quantum Dots
- •2.5 Fullerene
- •2.6 Carbon Nanohorns
- •2.7 Carbon Nano-Onions
- •2.8 Nano-Diamond
- •3. Supramolecular Chemistry in Drug Delivery
- •3.1 Principles of Supramolecular Chemistry
- •3.3 Applications of Supramolecular Biomaterials
- •4. Carbon Nanomaterial-Incorporated Supramolecular Drug Delivery
- •5.1 Cyclodextrins
- •5.2 Calixarenes
- •5.3 Cucurbituril
- •5.4 Pillarenes
- •5.5 Crown Ether
- •6. Toxicity Concerns of Carbon Nanomaterials
- •7. Improving the Effectiveness of Nanoparticle Systems
- •8. Future of Nanomedicine
- •9.1 Challenges
- •9.2 Future Perspectives and Opportunities
- •9.3 Conclusions
- •References
- •Carbon Nanomaterial-Based Polymeric Nanocomposites for Drug Delivery
- •1. Introduction
- •2.1 Carbon Quantum Dot-Based Polymer Nanocomposite
- •2.2 Carbon Nanotube-Based Polymer Nanocomposite
- •2.3 Graphene Quantum Dot-Based Polymer Nanocomposite
- •2.5 Fullerene-Based Polymer Nanocomposite
- •2.6 Nanodiamond-Based Polymer Nanocomposite
- •3. Drug Delivery Systems Using Carbon Nanomaterial
- •3.1 Anticancer Drug Delivery
- •3.3 Infectious Disease Drug Delivery
- •3.4 Topical Drug Delivery
- •3.5 Brain Drug Delivery
- •3.6 Oral Drug Delivery
- •4. Challenge and Future Perspectives
- •5. Conclusion
- •References
- •Carbon Nanomaterial-Incorporated Polysaccharide-Based Nanocomposite for Drug Delivery
- •1. Introduction
- •1.1 Drug Delivery
- •1.2 Carbon Nanomaterials
- •1.3 Polysaccharide-Based Nanocomposite
- •2.1 CN-Incorporated Alginate-Based Nanocomposite
- •2.2 CN-Incorporated Cellulose-Based Nanocomposite
- •2.3 CN-Incorporated Chitosan-Based Nanocomposite
- •2.4 CN-Incorporated Dextran-Based Nanocomposite
- •2.5 CN-Incorporated Hyaluronic Acid-Based Nanocomposite
- •2.6 CN-Incorporated Starch-Based Nanocomposite
- •2.7 CN-Incorporated Pectin-Based Nanocomposite
- •2.8 CN-Incorporated Guar Gum-Based Nanocomposite
- •2.9 CN-Incorporated Agarose-Based Nanocomposite
- •2.10 CN-Incorporated Carrageenan-Based Nanocomposite
- •2.11 CN-Incorporated Glucomannan-Based Nanocomposite
- •3. Challenges and Future Prospective
- •4. Concluding Remarks
- •References
- •Graphene-Based Nanomaterials for Drug Delivery
- •1. Introduction
- •1.1 Challenges in Conventional Drug Delivery Systems
- •1.2 Overview of Nanomaterials for Drug Delivery
- •1.3 Role of Graphene-Based Nanomaterials in Drug Delivery
- •2. Synthesis of Graphene
- •2.1 Chemical Reduction Method
- •2.2 Thermal Reduction
- •2.3 Electrochemical Reduction
- •2.4 Chemical Vapor Deposition Method
- •2.5 Mechanical Exfoliation
- •2.6 Epitaxial Growth Method
- •2.7 Growth in Solvothermal and Hydrothermal Systems
- •2.8 Electrochemical Deposition
- •3. Types of Graphene-Based Materials
- •3.1 Graphene Quantum Dots, (GQDs)
- •3.2 Graphene Oxide (GO)
- •3.3 Graphene Nanoribbons (GNRs)
- •3.4 Oxidized Graphene Nanoribbons
- •4. Graphene Functionalized Materials for Drug Delivery
- •4.1 In Bone Tissue Regeneration
- •4.2 In Neural Regeneration
- •4.3 In Photodynamic and Photothermal Therapy
- •4.4 In Enhancing Cellular and Humoral Immunity
- •4.6 Miscellaneous
- •5. Challenges and Future Perspective
- •6. Conclusion
- •References
- •Carbon Quantum Dots Based Materials for Drug Delivery
- •1. Introduction
- •2. Synthesis Process of Carbon Quantum Dots
- •2.1 Top-Down Approaches
- •2.2 Bottom-Up Approaches
- •2.3 Microwave-Assisted Method
- •2.4 Electrochemical Method
- •2.5 Laser Ablation Method
- •2.6 Pyrolysis Method
- •2.7 Template-Assisted Method
- •4. Challenges and Future Perspective
- •5. Concluding Remarks
- •References
- •Carbon-based Nanocarriers for Sustained Drug Release in Dentistry
- •1. Introduction
- •2.1 Oral Mucosa Structure
- •2.2 Sites for Drug Delivery
- •2.3 Permeability
- •3. Local Drug Delivery for Dental Diseases
- •3.1 Odontogenic Infection
- •3.2 Non-odontogenic Infection
- •4. Bio-adhesive Nanoparticles: Novel Treatment Modality
- •4.1 Bio-adhesive Nanoparticles
- •4.2 Mechanism of Bioadhesion
- •5.1 Carbon Nanotubes
- •5.2 Graphene
- •5.3 Nanodiamonds
- •5.4 Fullerenes
- •5.5 Porous Carbon
- •5.6 Carbon Dots
- •6. Drug Delivery Systems Based on CBNs
- •6.2 Immediate Drug Delivery System (IDDS)
- •6.3 Sustained-release Drug Delivery Systems
- •6.4 Controlled Drug Delivery System (CDDs)
- •8. Conclusion
- •References
- •Fullerene Based Materials for Drug Delivery
- •1. Introduction
- •2. Types of Fullerene Derivatives
- •2.1 Exohedral Fullerene Derivatives
- •2.2 Endohedral Fullerene Derivatives
- •2.3 Surface Derivatized Fullerenes
- •3. Interaction of Fullerene Derivatives for Drug Delivery
- •4. Fullerene Based Materials for Drug Delivery
- •4.1 Nucleic Acid Delivery
- •4.2 Peptide Delivery
- •4.3 Topical Drug Delivery
- •4.4 Infectious Diseases Drug Delivery
- •4.5 Anticancer Drug Delivery
- •4.7 Brain Drug Delivery
- •4.8 Ocular Drug Delivery
- •5. Challenges and Future Perspectives
- •6. Concluding Remarks
- •6.1 Abbreviations
- •References
- •Graphene Quantum Dots-based Nanomaterials for Drug Delivery
- •1. Introduction
- •2. Synthesis of GQDs
- •3. GQD’s Properties for Drug Delivery
- •3.1 Optical Properties
- •3.2 Physicochemical Properties
- •3.3 Mechanical Properties
- •3.4 Biocompatibility and Cytotoxicity
- •4. Characterization of GQDs-Based Nanomaterials
- •4.1 Characterization of Multifunctional GQDs-Based Nanomaterials
- •5.1 Strategies for Developing Medication Delivery Systems Based on GQD
- •5.2 PH-responsive Drug Delivery Systems (GQD-DDSs)
- •5.3 Targeted Drug Delivery Using Ligand-Based GQDs as a Mediator
- •5.4 Improvement of Medicines’ Pharmacological Properties Using GQDs
- •5.5 Enhancing Cytotoxicity with GQD-DDS
- •7. Applications of Chiral GQDs
- •10. Challenges and Future Perspectives
- •11. Conclusions
- •References
- •Carbon Nano-onions for Drug Delivery
- •1. Introduction
- •2. Carbon Nano-Onion: A Multi-Layered Nanocarrier
- •3. Synthesis of Carbon Nano-Onions
- •3.1 Annealing Method
- •3.2 Carbon Ion Implantation Method
- •3.3 Arc Discharge Method
- •3.4 Carbon Vapour Deposition Method
- •3.5 Pyrolysis Method
- •6. Carbon Nano-Onions in Drug Delivery
- •6.1 Delivery of Therapeutic Agents
- •6.2 Delivery of Targeting Agents
- •6.3 Delivery of Imaging Agents
- •7. Challenges and Future Perspectives
- •8. Concluding Remarks
- •References
- •Chitosan/Carbon Nanocomposites in Drug Delivery and Cardiovascular Diseases
- •1. Introduction
- •1.1 Drug Delivery
- •1.2 Cardiovascular Diseases
- •1.3 Chitosan and Its Properties
- •1.4 Chitosan/Carbon Nanocomposites
- •2. Chitosan/Carbon Nanocomposites in Drug Delivery
- •3. Chitosan/Carbon Nanocomposites in CVDs
- •3.1 Chitosan-Based Scaffolds
- •3.2 Chitosan in Cardiac Tissue Engineering
- •3.3 Chitosan-Based Cell Therapy
- •3.4 Chitosan-Based Gene Delivery
- •3.5 Chitosan-Protein Interaction
- •4. Challenges and Future Perspective
- •5. Concluding Remarks
- •References
- •Graphene Reinforced Chitosan Nanocomposites for Drug Delivery
- •1. Introduction
- •2. Chitosan: Structure and Properties
- •3. Graphene: Structure, Types and Properties
- •4.1 Electrospinning Method
- •4.2 Sol–gel Method
- •4.3 Solution Mixing Method
- •4.4 In-situ Polymerization Method
- •5.2 Chitosan/Graphene Aerogels
- •5.3 Chitosan/Graphene Hydrogels
- •5.4 Chitosan/Graphene Thin Films
- •6.1 Oral Drug Delivery
- •6.2 Mucosal Drug Delivery
- •6.3 Transdermal Drug Delivery
- •6.4 Parenteral Drug Delivery
- •7. Challenges and Future Perspectives
- •8. Concluding Remarks
- •References
- •1. Introduction
- •2. Functionalization of CNFs
- •2.1 The Need for Functionalization

Carbon Nano-onions for Drug Delivery 405
exploited as drug delivery targets (Fig. 13.6). The idea behind this is that the nanoonion’s layers can be created to have particular chemical characteristics, with such
affinity for a particular kind of cell or tissue. The medicine can be given precisely
to the target cells or tissue by being encapsulated within the nano-onion. Increased
medication bioavailability, less toxicity to organs other than the target, and enhanced
pharmacokinetics are benefits of utilizing nano-onions as targeting agents. However,
there may be certain disadvantages, such as the difficulty in producing and characterizing the nanoparticles and the possibility of immunogenicity. A noteworthy
example is the development of hyaluronic acid-conjugated carbon nanomaterials for
improved tumor targeting ability [58, 59]. Targeting tumor cells that overexpress
the CD44 + receptor with chemo and photo thermal therapy uses hyaluronic acid.
Carbon nanomaterial (CNM) carriers can effectively carry anticancer medications,
such as doxorubicin and gemcitabine, to the tumor locations, thanks to HA-targeting
hybrid systems. Using hyaluronic acid, carbon nano-onions have shown to be quite
promising for the delivery of specific drugs [60]. A HA-phospholipid compound was
used in the work by d’Amor et al. to target cancer cells that overexpress CD44 while
improving the solubility of the nanostructure. In comparison to human ovariancancer
cells with undetectable levels of CD44, non-covalently functionalized carbon nanoonions with HA-phospholipids conjugate exhibit outstanding in vitro cell survival
in human breast carcinoma cells [61]. Additionally, they have a high level of in vivo
biocompatibility in zebrafish (Daniorerio) at various developmental stages and are
mostly found in the digestive system of zebrafish larvae. Mamidi et al. discovered
that the nano-onions complex with other nanoparticles might thrive as a viable pH
and temperature-triggered drug delivery platform for GI tract and colon focused
drug delivery [62]. There are various instances of nanocarrier systems on the market
that have received FDA approval, demonstrating the effectiveness of the nanocarrier
method in this regard. This viewpoint confirms that carbon nano-onions have the
potential to serve as nanocarriers for the delivery of drugs. Already described are
the many standards and factors to take into account when constructing a nanocarrier
[18].
6.3 Delivery of Imaging Agents
A chemical called an imaging agent is used to improve the image quality in medical
imaging procedures like computed tomography and magnetic resonance imaging,
among others. The potential for using nano-onions, which are microscopic particles
comprised of concentric layers of carbon, as imaging agents has been investigated.
The idea behind employing nano-onions as imaging agents is that they are capable
of being functionalized with targeting molecules like antibodies or peptides, which
can then bind specifically to sick cells or tissues [63]. This makes it possible to image
the targeted area of interest with greater accuracy and precision. Encapsulating the
imaging agent within the onion-like structure’s layers at the nanoscale level, which
can then be coated with a biocompatible substance to prevent degradation and boost

406 S. Yasri and V. Wiwanitkit
Fig. 13.6 Ta rge t ing an d
imaging conjugate of
nano-onion
stability,is the first step in the delivery of imaging agents utilizing nano-onions. Nanoonions are advantageous as imaging agents due to their small size, which enables
them to reach deep within tissues and organs, biocompatibility, and potential for multi
functionalization. Cons include possible toxicity and difficulties with production
scaling up and manufacturing. However, work is still being done to overcome these
obstacles and boost the efficiency of nano-onions as imaging agents. At present, there
are some reports on the application of nano-onions on this specific purpose. The good
examples are the reports on application for imaging several cancers [64, 65]. The
applications of fluorescent nano-onions are the new hope in clinical medicine for
management of several disorders (Fig. 13.7).
There are several fascinating reports on the use of nano-onions for imaging agent
delivery. First, Bowman et al. reported that onion-like carbon is used in engineered
three-dimensional breast tumor models composed of phantom tissue mimicking infiltrating ductal carcinoma surrounded by phantom tissue mimicking healthy fibro
glandular tissue due to its strong interaction with terahertz frequencies and ability
to be activated for selective binding to cancer cells. Bowman et al. reported that
this model is scanned utilizing the terahertz reflection mode to test the efficiency of
contrast agents for tissue differentiation. A 10% concentration of onion-like carbon
has the greatest impact on the terahertz signal in both spectroscopy and imaging and
offers promise as a terahertz contrast agent [64]. Another study by Bartelmess et al.
[65], was found that the addition of a terminal bromo substituent allows the fluorophore to be immobilized on the surface of carbon nano-onions, resulting in potential

Carbon Nano-onions for Drug Delivery 407
Fig. 13.7 Clinical applications of fluorescent nano-onion in clinical medicine
imaging agents for biological and biomedical applications. Sun et al. created waterdispersible carbon nano-onion clusters with an average hydrodynamic size of 90 nm
by simply sonicating candle soot in an oxidizing acid combination. They discovered
that following intravenous delivery, the complex can be employed for photothermal/
photoacoustic dual-modal imaging-guided photothermal therapy. Furthermore, the
complex may be eliminated from the mouse body in less than a week, providing its
long-term biosafety [66].
7 Challenges and Future Perspectives
Due to their distinct physicochemical characteristics, high surface area, biocompatibility,and low t oxicity, carbon nano-onions have become a potential material for drug
delivery. However, there are still some issues and considerations for the future that
must be addressed. The production of carbon nano-onions with controlled s ize, shape,
and functionalization is one of the key difficulties. The majority of current synthesis
techniques rely on thermally processing carbon precursors, which can produce a
variety of forms and sizes. Additionally, functionalizing carbon nano-onions with
medicinal compounds or targeted ligands is still a challenging task that has to be
developed further. Understanding how carbon nano-onions interact with biological
systems is another difficult task. Although carbon nano-onions are regarded biocompatible, their in vivo behavior is still unknown. Furthermore, the mechanisms of
cellular absorption and intracellular trafficking of carbon nano-ions must be understood. Carbon nano-onions have the potential to transform medication delivery by

408 S. Yasri and V. Wiwanitkit
enabling focused therapy, controlled release, and imaging in the future. Furthermore, their distinct features could be used in other biological applications like as
tissue engineering and biosensing. Finally, carbon nano-onions have demonstrated
remarkable potential as a medium for future drug delivery.
8 Concluding Remarks
To summarize, carbon nano-onions are a potential and novel strategy to drug delivery,
with their unique structure and physicochemical features allowing for enhanced
drug targeting and release. These nanoparticles’ prospective applications in several
disciplines of medicine, including cancer therapy, are particularly fascinating. More
research is needed, however, to completely understand the biological interactions and
toxicity of carbon nano-onions, as well as to improve their designs for specific drug
delivery applications. Overall, the invention of carbon nano-onions for drug delivery
is a significant step toward more effective and tailored treatments for a variety of
ailments.
Conflict of Interest Authors declare no conflict of interest.
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Chitosan/Carbon Nanocomposites in Drug Delivery and Cardiovascular Diseases
Ayman M. Mahmoud, Ahmed M. Sayed, Emad H. M. Hassanein,
Krishna Manjari Sahu, and Sarat Kumar Swain
Abstract Controlled and sustainable delivery of therapeutics for accurate adminis-
tration at requisite location with proper number of dosages are essential to treat
diverse fatal diseases by reducing patient complications and improving safety
concerns related to drug administration. Cardiovascular diseases (CVDs) are a class
of serious disorders that represent the leading cause of mortality worldwide. Chitosan
(CS) is a natural and biocompatible polysaccharide that shows promising properties
in various fields, namely, drug, gene, and therapeutic proteins delivery, and the fabrication of scaffolds and hydrogels for tissue engineering. It exhibits structural similarities with glycosaminoglycans which represent the main component of the extracellular matrix (ECM), and hence possesses great potential for tissue engineering and
other therapeutic purposes. CS possesses fascinating mechanical properties but poor
electrical properties, therefore several modifications have been performed to enhance
the electrical properties of CS-based scaffolds. To modify the characteristic features
of CS, carbonaceous nanomaterials like carbon nanotube (CNT), graphene, carbon
dot, carbon nanohorn (CNH), carbon nano-onion (CNO) and nanodiamond (ND) are
effectively implemented. This chapter introduces the recent findings, latest developments, and innovations in the use of CS/carbon nanocomposite in drug delivery and
treatment of CVDs. The beneficial effects of CS/carbon nanocomposite in cardiac
tissue engineering, cell therapy, gene delivery, and its interaction with proteins are
also discussed in this chapter.
A. M. Mahmoud (B)
Department of Life Sciences, Faculty of Science and Engineering, Manchester Metropolitan
University, Manchester, UK
e-mail: a.mahmoud@mmu.ac.uk
A. M. Sayed
Biochemistry Laboratory, Chemistry Department, Faculty of Science, Assiut University, Assiut,
Egypt
E. H. M. Hassanein
Department of Pharmacology and Toxicology, Faculty of Pharmacy, Al-Azhar University, Assiut,
Egypt
K. M. Sahu · S. K. Swain (
Veer Surendra Sai University of Technology, Burla, Sambalpur, India
e-mail: skswain_chem@vssut.ac.in
B
)
413

414 A. M. Mahmoud et al.
Keywords Carbonaceous nanomaterials · Chitosan · Cardiovascular diseases ·
Cardiac tissue engineering · Drug delivery
Abbreviations
1
H NMR Proton nuclear magnetic resonance
5-FU 5-Fluorouracil
AFM Atomic force microscopy
AGO Amine functionalized Graphene oxide
Apt Aptamer
ATR-IR Attenuated total reflectance- infrared Spectroscopy
C
60
CMC Carboxymethyl cellulose
CMCS Chemically modified chitosan
CS Chitosan
DCA-HPCHS Mphiphilic deoxycholic acid modified-hydropropyl chitosan
DOX Doxorubicin
FA Folic acid
FA-COS Folic acid–chitosan oligosaccharide conjugate
FTIR Fourier transform infrared Spectroscopy
GC
1
HA
1
HPLC High-performance liquid chromatography
MOFs Metal organic framework
ND-OH Hydroxylated nanodiamond
OCMC O-carboxymethyl chitosan
SEM Scanning electron microscope
SWNH Single-walled carbon nanohorns
TEM Transmission electron microscope
TTP Tripolyphosphate
UPLC Ultra performance liquid chromatography
UV-Vis UV–vis spectrophotometer
XRD X-ray diffractometer
C60fullerene
Galactosylated chitosan
Hydroxyapatite
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